At initial assessment, mild developmental delay was noted. Noonan syndrome was suspected. Echocardiography showed a small perimembranous VSD and nonobstructive HCM with mild mitral valve prolapse.

Noonan syndrome is a genetic condition that affects around 1 in every 1,000–2,500 people. The signs and symptoms can vary greatly from person to person, so this condition may be underdiagnosed ...

Noonan syndrome is a genetic disorder that affects ... Normal cardiac function was restored after medication and treatment. An echocardiogram revealed a structurally normal heart with normal ...

Worried, her parents took her to the emergency room. There doctors discovered that Maria, who at age 2 was diagnosed with Noonan syndrome, a genetic disorder that can lead to several health issues ...

In Noonan syndrome, Sogroya achieved 10.4 cm/year height gain vs 9.2 cm/year with daily somatropin. Unlock your all-in-one trading dashboard with real-time alerts, rankings, and stock ideas—60% ...

The Danish pharmaceutical giant said the drug was more effective than a daily growth hormone in children with Noonan syndrome--a genetic condition that stops typical development in some parts of ...

One is known as cardio-facio-cutaneous, or CFC, syndrome, for which she and her team discovered the genes responsible last year. The other two are called Noonan syndrome and Costello syndrome. In a ...

A 64-year-old man with Noonan syndrome presented to the emergency department with a 1-day history of abdominal pain, nausea, vomiting, decreased oral intake, and obstipation. His abdomen was ...

To the best of our knowledge, there have been no previously published reports in the medical literature of phytobezoars in patients with Noonan syndrome. This case represents what may be an ...